Related Experiment Video
Updated: Jan 19, 2026

Fabrication of White Light-emitting Electrochemical Cells with Stable Emission from Exciplexes
Published on: November 15, 2016
Fluorescence Properties and Exciplex Formation of Emissive Naphthyridine Derivatives: Application as Sensors for
Junko Hirota1, Kazuteru Usui2, Yasufumi Fuchi2
1Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
Abstract:
Water-soluble donor-acceptor-type fluorophore 15Nap-Cl having two trifluoromethyl groups and a Cl group on a 1,5-aminonaphthyridine framework was prepared. Fluorophore 15Nap-Cl showed strong solvatochromic fluorescence, and, as the solvent polarity increased, a bathochromic shift was observed accompanied by an increase in the fluorescence quantum yield. In addition, in the presence of amines such as ethylamine, diethylamine, and aniline, further considerable bathochromic shifts in the fluorescence were observed. Density functional calculations identified the source of the fluorescence behavior as exciplex formation between 15-Nap-Cl and the corresponding amine. The fluorescence behavior was exploited to fabricate a sensor that can identify various primary, secondary, and tertiary amines.
Related Concept Videos
05:51Fabrication of White Light-emitting Electrochemical Cells with Stable Emission from Exciplexes
Physical Properties of Amines
16:19Synthesis, Cellular Delivery and In vivo Application of Dendrimer-based pH Sensors
07:21Fibroblast-Derived 3D Matrix System Applicable to Endothelial Tube Formation Assay
09:46Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores
Aldehydes and Ketones with Amines: Imine Formation Mechanism
Imines are formed under mildly acidic conditions. A pH of 4.5 is ideal for the reaction.
If the pH is low or the solution is too acidic, the reaction slows down in the...
